标题
The expanding family of hypophosphatemic syndromes
作者
关键词
-
出版物
JOURNAL OF BONE AND MINERAL METABOLISM
Volume 30, Issue 1, Pages 1-9
出版商
Springer Nature
发表日期
2011-12-13
DOI
10.1007/s00774-011-0340-2
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- An Atypical Degenerative Osteoarthropathy in Hyp Mice is Characterized by a Loss in the Mineralized Zone of Articular Cartilage
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- Tumor-induced osteomalacia
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- Bone proteins PHEX and DMP1 regulate fibroblastic growth factor Fgf23 expression in osteocytes through a common pathway involving FGF receptor (FGFR) signaling
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- Fibroblast growth factor 23 regulates renal 1,25-dihydroxyvitamin D and phosphate metabolism via the MAP kinase signaling pathway in Hyp mice
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- FGF-23/Klotho signaling is not essential for the phosphaturic and anabolic functions of PTH
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- A clinician's guide to X-linked hypophosphatemia
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- Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets
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- A Loss-of-Function Mutation in NaPi-IIa and Renal Fanconi's Syndrome
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- Survey of the Enthesopathy of X-Linked Hypophosphatemia and Its Characterization in Hyp Mice
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- Isolated C-terminal tail of FGF23 alleviates hypophosphatemia by inhibiting FGF23-FGFR-Klotho complex formation
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- Calcimimetics as an Adjuvant Treatment for Familial Hypophosphatemic Rickets
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- A mouse model with postnatal endolymphatic hydrops and hearing loss
- (2008) Cliff A. Megerian et al. HEARING RESEARCH
- NHERF1Mutations and Responsiveness of Renal Parathyroid Hormone
- (2008) Zoubida Karim et al. NEW ENGLAND JOURNAL OF MEDICINE
- McCune-Albright syndrome
- (2008) Claudia E Dumitrescu et al. Orphanet Journal of Rare Diseases
- A translocation causing increased -Klotho level results in hypophosphatemic rickets and hyperparathyroidism
- (2008) C. A. Brownstein et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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